Personal Stories, • 6/24/24 In conversation with James Coney and Shaun Pye, a webinar for Rare Chromo Day 2025 Previous N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies Next Genomics England Research Seminar May 2024 - Yuyang Chen and Daniel Greene You Might Also Like Rare-X Launch De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin We Belong Together Dr Sarah Wynn - How the discovery of ReNU syndrome is impacting patients and families Professor Stephan Sanders - Clarifying the clinical picture of ReNU syndrome & looking to the future
Personal Stories, • 6/24/24 In conversation with James Coney and Shaun Pye, a webinar for Rare Chromo Day 2025 Previous N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies Next Genomics England Research Seminar May 2024 - Yuyang Chen and Daniel Greene You Might Also Like Rare-X Launch De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin We Belong Together Dr Sarah Wynn - How the discovery of ReNU syndrome is impacting patients and families Professor Stephan Sanders - Clarifying the clinical picture of ReNU syndrome & looking to the future
